| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7395022-7395209 | Common:4; Rare:58 | ||||
| chr19:7488988-7489053 | Rare:30 | ||||
| chr19:7506838-7507080 | Common:2; Rare:59 | ||||
| chr19:7522522-7522693 | Rare:63; Clinvar:2 | ||||
| chr19:7533848-7534213 | Common:3; Rare:95; Clinvar (benign):1 | ||||
| chr19:7535574-7535807 | Common:3; Rare:86 | ||||
| chr19:7550299-7550545 | Rare:70; Clinvar (benign):1 | ||||
| chr19:7629531-7629859 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636997-7637151 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr19:7903536-7903926 | Rare:127 | ||||
| chr19:7920234-7920482 | Rare:103 | ||||
| chr19:7943625-7943833 | Rare:60 | ||||
| chr19:8005519-8005821 | Common:1; Rare:105 | ||||
| chr19:8320859-8321031 | Rare:56 | ||||
| chr19:8321307-8321723 | Common:2; Rare:167 |